ライフサイエンスコーパス: blastocoel

1 in the vectorial transport of water into the blastocoel.

2 th secreted glypicans and coreceptors in the blastocoel.

3 and the ingression of surface cells into the blastocoel.

4 t 2 h after PMCs began to migrate within the blastocoel.

5 onfined to the polar region by the expanding blastocoel.

6 ized cells covering the inner surface of the blastocoels.

7 rospective primary mesenchyme cells into the blastocoel, after which they migrate and then fuse to fo

8 increase in the hydrostatic pressure of the blastocoel, an embryonic cavity in contact with the pros

9 stocoelar cells) are also present within the blastocoel and are migrating and fusing with one another

10 foxN2/3 morphant PMCs do not organize in the blastocoel and fail to join the PMC syncytium.

11 n C. elegans embryos involves formation of a blastocoel and the ingression of surface cells into the

12 ement of primary mesenchyme cells within the blastocoel and the shapes of the skeletal rods.

13 l cycle (32-cell stage) and ingress into the blastocoel at the 6th cycle (62-cell stage).

14 the zona pellucida (ZP), trophectoderm (TE), blastocoel (BC), and inner cell-mass (ICM), using subjec

15 uce trophoblast stem cells, trophectoderm or blastocoel cavities, and therefore do not implant into t

16 It faces the blastocoel cavity and later gives rise to the extraembry

17 zation using endocytosis of ligands from the blastocoel cavity as a positioning cue.

18 pective head mesoderm cells to appear in the blastocoel cavity at the onset of gastrulation, stage 10

19 While a blastocoel cavity formed and epithelial cell polarity wa

20 rbed when this antibody is injected into the blastocoel cavity indicating that IMZ cell interaction w

21 e of 3.9 +/- 3.6 Pa, relative to the central blastocoel cavity of the embryo, was found to be consist

22 ssively restricted to the PE adjacent to the blastocoel cavity together with the transcription factor

23 t of epithelial polarity and appearance of a blastocoel cavity.

24 marginal zone cells of the blastula into the blastocoel cavity.

25 cycle arrest in G2 phase, and eventually to blastocoel collapse, impaired NLS-mediated protein uptak

26 including the formation of an intercellular blastocoel, culminate in a morphological left-right asym

27 embryo volume and cell volume decrease, the blastocoel disappears, and 34.4% of the cell mass become

28 ary mesenchyme cells (PMCs) ingress into the blastocoel during an epithelial-to-mesenchymal transitio

29 vitation, as well as stimulating the rate of blastocoel expansion and increasing the number of trophe

30 P produced is used by the sodium pump during blastocoel expansion in the human and bovine blastocyst,

31 In Xenopus, the blastocoel-facing, basolateral surfaces where signaling

32 Never is the blastocoel filled by a mass of mesenchyme.

33 rive in part from cells at the centre of the blastocoel floor that express XHex, the Xenopus cognate

34 features of TE differentiation required for blastocoel formation include intercellular junction biog

35 is required to prevent oxidative stress when blastocoel formation is accompanied by increased oxidati

36 gesting that the PAR-3 protein has a role in blastocoel formation.

37 M and is detected at the very first signs of blastocoel formation.

38 itor W-7 exhibited a dose-dependent delay in blastocoel formation.

39 enuated the ionophore-induced stimulation of blastocoel formation.

40 ed Ca2+ signalling and a subsequent delay in blastocoel formation.

41 e apical or basal surfaces of cells prior to blastocoel formation; we demonstrate that this localizat

42 The blastocoel forms at the first cleavage division since fu

43 hesive interactions results in a loss of the blastocoel in early embryos and ripping of the ectoderma

44 Formation of the blastocoel in early Xenopus embryos was studied with a n

45 of this information on the oral side of the blastocoel in turn depends on Spdri expression in the or

46 Here, we report that the cleavage-stage blastocoel is traversed by hundreds of extremely long ce

47 iblast- and primitive endoderm-like cells, a blastocoel-like cavity and a trophectoderm-like outer la

48 Injection of hydrolytic sulfatase into the blastocoels of gastrula stage embryos resulted in severe

49 in PrE cells positioned in contact with the blastocoel, raising the possibility that these cells are

50 w been found to occur by invagination into a blastocoel, revealing an unanticipated embryological aff

51 In the blastocoel roof (BCR) of the Xenopus laevis embryo, epib

52 l tension promotes FN fibril assembly in the blastocoel roof (BCR), while reduced BCR tension inhibit

53 ir6.1 is localized to basal membranes on the blastocoel roof and cell-cell junctions.

54 o establish that radial intercalation in the blastocoel roof requires integrin-dependent contact of d

55 bronectin fibrils in vivo is correlated with blastocoel roof thickening and a loss of deep cell polar

56 ercalation movements, which are required for blastocoel roof thinning and epiboly.

57 Ectodermal cells from the blastocoel roof use alpha5beta1 integrins to assemble a

58 Head mesoderm migrates along the blastocoel roof, while trunk mesoderm undergoes converge

59 FN-dependent cellular rearrangements in the blastocoel roof.

60 the fibronectin matrix and thickening of the blastocoel roof.

61 essential for, mesoderm cell adhesion to the blastocoel roof.

62 ls and the cells of the substrate layer, the blastocoel roof.

63 Apoptotic cells accumulated in the blastocoel, suggesting that before the midblastula trans

64 zone adjacent to the interior margin of the blastocoel that is populated by cells derived from both

65 hogenesis, including PMC distribution in the blastocoel, the size of the skeleton and its branching p

66 Cells that ingress into the blastocoel undergo an apical flattening associated with

67 archenteron as well as in other areas of the blastocoel wall.

68 es as a polarized epithelium adjacent to the blastocoel, with a basement membrane separating it from